《Synthesis of protected α-amino acids via decarboxylation amination from malonate derivatives》 was published in Organic & Biomolecular Chemistry in 2020. These research results belong to Fu, Hui; Li, Peihe; Wang, Zheng; Li, Xiaoying; Dai, Qipu; Hu, Changwen. Related Products of 36016-38-3 The article mentions the following:
A general and efficient strategy for the synthesis of protected α-amino acids is reported. The method uses malonate derivatives as the starting materials and Cs2CO3 as a base at 60 degrees, giving α-amino acid derivatives in moderate yields by releasing CO2. This methodol. shows broad substrate scope (primary and secondary acids), excellent functional group tolerance and high efficiency to give the desired products under mild reaction conditions. It also allows the construction of β and γ-amino acids and other unnatural products. After reading the article, we found that the author used N-tert-Butoxycarbonylhydroxylamine(cas: 36016-38-3Related Products of 36016-38-3)
N-tert-Butoxycarbonylhydroxylamine(cas: 36016-38-3) belongs to anime. Left-handed and right-handed forms (mirror-image configurations, known as optical isomers or enantiomers) are possible when all the substituents on the central nitrogen atom are different (i.e., the nitrogen is chiral). With amines, there is extremely rapid inversion in which the two configurations are interconverted.Related Products of 36016-38-3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics